Synthesis of the Thiazole–Thiazoline Fragment of Largazole Analogues
作者:Frederik Diness、Daniel S. Nielsen、David P. Fairlie
DOI:10.1021/jo201675r
日期:2011.12.2
fragment of the marinenaturalproduct largazole, a potent histone deacetylase 1 inhibitor, has been synthesized in five steps. The methodology provides rapid access to thiazole-4-carbonitrile, thiazole-4-carbimidate, thiazole–oxazoline, and other thiazole–thiazoline derivatives that are important intermediates in the totalsynthesis of many naturalproducts with important biological properties.